Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey

Author:

Grasso Fiorentino1ORCID,Cirillo Emilia1,Quaremba Giuseppe2,Graziano Vincenzo2,Gallo Vera1,Cruoglio Letizia3,Botta Carmine4,Pignata Claudio1ORCID,Motta Sergio3

Affiliation:

1. Department of Translational Medical Sciences, Pediatric section; Federico II University; Naples Italy

2. Department of Advanced Biomedical Sciences; Federico II University; Naples Italy

3. Department of Neurosciences, Reproductive and Odontostomatological Sciences; Federico II University; Naples Italy

4. Department of Morphologic and Functional Diagnostics, Radiotherapy and Legal Medicine; Federico II University; Naples Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. Variation in tonsil size in 4- to 17-year-old schoolchildren;Akcay;The Journal of Otolaryngology,2006

2. Severe combined immunodeficiences: new and old scenarios;Aloj;International Review of Immunology,2012

3. Clinical features of 78 adults with 22q11 deletion syndrome;Bassett;American Journal of Medical Genetics. Part A,2005

4. Modern assessment of tonsils and adenoids;Brodsky;Pediatric Clinics of North America,1989

5. Adenoid tissue rhinopharyngeal obstruction grading based on fiberendoscopic findings: A novel approach to therapeutic management;Cassano;International Journal of Pediatric Otorhinolaryngology,2003

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